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Clinical Trial Summary

Phase 1b: To evaluate the safety and tolerability of multiple ascending doses of efavaleukin alfa in subjects with steroid refractory chronic graft versus host disease (cGVHD). Phase 2: To evaluate the efficacy of efavaleukin alfa in subjects with steroid refractory cGVHD as measured by overall response rate (ORR) at 16 weeks according to the 2014 cGVHD NIH Consensus Criteria. Due to early termination, the Phase 2 portion of this study was not conducted.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03422627
Study type Interventional
Source Amgen
Contact
Status Terminated
Phase Phase 1/Phase 2
Start date April 27, 2018
Completion date October 13, 2022